Comparison of the large subunit ribosomal DNA of Neospora and toxoplasma and development of a new genetic marker for their differentiation based on the D2 domain

• Published in: Molecular and cellular probes Vol. 12; no. 1; pp. 1 - 13
• Main Authors: Ellis, J T, Amoyal, G, Ryce, C, Harper, P A, Clough, K A, Homan, W L, Brindley, P J
• Format: Journal Article
• Language: English
• Published: England 01.02.1998
• Subjects: Animals; Base Sequence; DNA Primers; DNA, Protozoan - chemistry; DNA, Ribosomal - chemistry; Genetic Markers; Macromolecular Substances; Molecular Sequence Data; Neospora - genetics; Polymerase Chain Reaction; Sequence Alignment; Sequence Homology, Nucleic Acid; Toxoplasma - genetics
• ISSN: 0890-8508; 1096-1194
• DOI: 10.1006/mcpr.1997.0143

The latest release of the large subunit ribosomal database contains 429 sequences, yet only 10 (six nuclear and four mitochondrial) are derived from parasites of the phylum Apicomplexa. Three of these (all Toxoplasma gondii) were previously contained in the 1994 release of the database. As an initiative towards an understanding of ribosomal gene organization in the Apicomplexa, the primary sequence of the large subunit (LSU) rDNA of Neospora caninum is presented, and compared with a consensus sequence derived for the LSU rDNA of T. gondii. Nucleotide differences observed between these two taxa in the D2 expansion segment (or domain) (also called the C1/C1' region) of the LSU rDNA were incorporated into a primer that forms the basis of a species-specific polymerase chain reaction (PCR) for N. caninum. The D2 domain of the LSU rDNA, therefore, represents a new genetic marker that can be used for the differentiation and identification of Neospora from other cyst-forming coccidia.